Associated Papers
Identification of novel and recurrent mutations in nicotinamide nucleotide transhydrogenase (NNT) underlying familial glucocorticoid deficiency-type 4 in multiple Saudi families.
Alwan IA et al.
Journal of Clinical & Translational Endocrinology, 2026
Lack of NAD(P)+ transhydrogenase activity in patients with primary adrenal insufficiency due to NNT variants.
Francisco A et al.
European Journal of Endocrinology, 2024
Select a paper to view details